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EP0248183A1 - Polyesterpolyols liquides à température de chambre à base de 2-méthyl-butanediol-1,4, leur procédé de préparation et leur utilisation pour la préparation de matières plastiques par le procédé de polyaddition de polyisocyanate - Google Patents

Polyesterpolyols liquides à température de chambre à base de 2-méthyl-butanediol-1,4, leur procédé de préparation et leur utilisation pour la préparation de matières plastiques par le procédé de polyaddition de polyisocyanate Download PDF

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Publication number
EP0248183A1
EP0248183A1 EP87105757A EP87105757A EP0248183A1 EP 0248183 A1 EP0248183 A1 EP 0248183A1 EP 87105757 A EP87105757 A EP 87105757A EP 87105757 A EP87105757 A EP 87105757A EP 0248183 A1 EP0248183 A1 EP 0248183A1
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EP
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Prior art keywords
weight
methyl
butanediol
polyester polyols
mixture
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EP87105757A
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German (de)
English (en)
Inventor
Joachim Dr. Steu
Wolfgang Dr. Straehle
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BASF SE
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BASF SE
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
    • C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds

Definitions

  • polyester polyols and their use for the production of polyurethane plastics by the polyisocyanate polyaddition process is known and is described in numerous literature and patent publications. For example, we would like to refer to the Kunststoff-Handbuch, Volume 7, Polyurethane, 1st edition, 1966, published by A. Höchtlen and R. Vieweg, and 2nd edition, 1983, published by G. Oertel, Carl Hanser Verlag, Kunststoff, Vienna.
  • the polyester polyols are usually prepared from polycarboxylic acids and polyhydric alcohols by melt condensation in the presence of acids or metal salts as a catalyst.
  • the polycondensation is expediently carried out under reduced pressure in order to distill off the water formed during the condensation from the reaction mixture and to shift the equilibrium reaction in the direction of the polyester formation. In this way, for example, polyester polyols with acid numbers greater than 5 can be produced in relatively short reaction times.
  • polyester polyols in particular those based on adipic acid and alkanediols, alkanediol mixtures or mixtures of alkanediols and higher alcohols, are used in large quantities for the production of polyurethane plastics for a large number of applications, the products also have disadvantages.
  • a particular disadvantage is that the polyester polyols crystallize completely or partially under normal storage conditions or have such a high viscosity that they cannot be processed directly at room temperature using conventional polyisocyanate polyaddition processes.
  • the polyester polyols usually have to be melted and homogenized in explosion-proof apparatus and can only be reacted at elevated temperatures in expensive temperature-controlled devices. This makes the manufacture of finished polyurethane parts more expensive.
  • liquid polyester polyols with hydroxyl numbers from 40 to 80 which are obtained by polycondensation of organi Dicarboxylic acids with polyol mixtures of at least four di- and trihydric alcohols based on 1,4-butanediol, 1,6-hexanediol, 1,5-pentanediol and / or diethylene glycol and an alkanetriol, such as glycerol and / or trimethylolpropane , in certain defined proportions.
  • polyurethane elastomers obtained in this way have an extraordinarily favorable low-temperature behavior and excellent hydrolysis resistance with high mechanical strength as well as a very good compression set and the flexible polyurethane foams have, in addition to improved hydrolysis resistance, very good punchability.
  • polyol mixtures of the type mentioned are relatively expensive since the structural components are obtained in part by reducing the corresponding dicarboxylic acid mixtures and are only available in limited amounts for the production of polyester polyols.
  • the polycondensation reaction requires a certain technical skill.
  • pigmentable unsaturated polyester resin compositions with low shrinkage are also known, which as a glycol component is a mixture of 15 to 70 mol% neopentyl glycol and 10 to 30 mol% 2,2-bis Contain (4-hydroxycyclohexyl) propane and where the glycol component can have 1 to 15 mol% of an additional polyhydric alcohol.
  • a glycol component is a mixture of 15 to 70 mol% neopentyl glycol and 10 to 30 mol% 2,2-bis Contain (4-hydroxycyclohexyl) propane and where the glycol component can have 1 to 15 mol% of an additional polyhydric alcohol.
  • 2-methyl-butanediol-1,4 is also mentioned for this purpose.
  • the object of the present invention was to develop polyester polyols which are as low-viscosity as possible and which are liquid at room temperature and which can be processed on conventional devices without problems using the polyisocyanate polyaddition process to give compact or cellular plastics having a good level of mechanical properties.
  • the invention thus relates to liquid at 25 ° C, units with the structure -OCH2-CH (CH3) -CH2-CH2O- containing polyester polyols, which are prepared by melt condensation of aliphatic polycarboxylic acids and / or polycarboxylic acid derivatives and at least one polyhydric aliphatic Alcohol in the presence or absence of esterification catalysts and characterized in that 2-methyl-butanediol-1,4 or mixtures of 2-methyl-butanediol-1,4 and at least one linear or branched, aliphatic 2 - Up to 4-valent alcohol with a 2-methyl-butanediol 1,4-content of at least 20 wt .-% before preferably 40 to 80% by weight, based on the weight of the alcohol mixture.
  • the invention further relates to a process for the preparation of liquid at 25 ° C, units having the structure -OCH2-CH (CH3) -CH2-CH2O- containing polyester polyols according to claim 6 and the use of the polyester polyols according to the invention 1 for the production of compact or cellular polyurethane or polyurethane-polyurea plastics, preferably of compact or cellular polyurethane elastomers, according to the polyisocyanate polyaddition process according to claim 10.
  • the polyester polyols according to the invention have an average functionality of from 2 to 3, preferably from 2 to 2.5, a hydroxyl number from 25 to 300, preferably from 40 to 80 for elastic, from 80 to 160 for semi-hard and from 160 to 300 for hard Plastics, an acid number of less than 2 mg KOH / g, preferably less than 1 mg KOH / g and in particular from 0.9 to 0.2 mg KOH / g, and a viscosity at 25 ° C of 200 to 105, preferably of 800 to 20,000 m.Pa.s.
  • Compact or cellular polyurethanes or polyurethane-polyurea plastics produced from the polyester polyols according to the invention - hereinafter referred to as PU or PU-PH plastics - have a high level of mechanical properties for numerous technical applications and are particularly characterized by good hydrolysis stability and compatibility with inert physical blowing agents.
  • the polyester polyols according to the invention are produced by polycondensation of aliphatic polycarboxylic acids and / or aliphatic polycarboxylic acid derivatives, preferably aliphatic dicarboxylic acids having 2 to 12 carbon atoms, in particular 4 to 6 carbon atoms in the alkylene radical and 2-methyl-butanediol-1,4 or mixtures of 2-methyl 1,4-butanediol and at least one branched, preferably linear aliphatic, preferably linear, aliphatic, 2- to 4-valent, preferably 2- to 3-valent alcohol, wherein the mixture contains at least 20% by weight of 2-methyl-butanediol 1.4, in the absence or preferably in the presence of customary known esterification catalysts.
  • Suitable aliphatic dicarboxylic acids are: dodecanedio, undecandi, sebacic, azelaic, cork, pimelic, adipic, glutaric, succinic, malonic and oxalic acid.
  • the corresponding dicarboxylic anhydrides e.g. Succinic anhydride, or mono- and / or dicarboxylic acid esters with low molecular weight alcohols, for example those with 1 to 4 carbon atoms, preferably 1 to 2 carbon atoms in the alkyl radical, such as e.g. the dicarboxylic acid mono- or dimethyl esters, ethyl esters, etc.
  • the aliphatic dicarboxylic acids and / or derivatives can also be used individually or as mixtures.
  • Mixtures of succinic acid, glutaric acid and adipic acid are preferably used, advantageously in weight ratios of 20 to 35: 35 to 50: 20 to 32 and in particular adipic acid.
  • aliphatic 2- to 4-valent alcohols are used to form the mixture: branched and / or preferably linear alkanediols having 2 to 12 carbon atoms, preferably 2 to 6 carbon atoms in the alkylene radical, polyoxyalkylene diols , advantageously those based on 1,2-propylene oxide and / or ethylene oxide with a molecular weight from 106 to 622, preferably from 106 to 262, linear or branched alkane triols having 3 to 6 carbon atoms and / or pentaerythritol.
  • alkanediols such as, for example, 2,2-dimethyl-1,3-propanediol, 2,2,4-trimethyl-1,6-hexanediol, 1,3-butanediol, ethanediol, 1,2- or 1,3 Propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,10-decanediol and 1,12-dodecanediol, polyoxyalkylene diols, such as, for example, diethylene glycol, trioxyethylene -glycol, tetraoxyethylene glycol and higher molecular weight polyoxyethylene glycols, dipropylene glycol, trioxypropylene glycol, tetraoxypropylene glycol and higher molecular weight polyoxypropylene glycols as well as polyoxypropylene
  • the polyhydric aliphatic alcohols can be used individually or in the form of mixtures.
  • the alcohol mixtures consist of 20 to approximately 100% by weight, preferably 40 to 80% by weight, 2-methyl 1,4-butanediol and 80 to about 0% by weight, preferably 20 to about 60% by weight, of at least one linear or branched aliphatic alcohol which may have ether bridges.
  • esterification catalysts which can be used are, for example, iron, cadmium, cobalt, lead, zinc, antimony, magnesium, titanium and tin catalysts in the form of metals, metal oxides or salts.
  • Tin salts e.g. according to US 3 162 616, tin dioctoate and / or tetrabutyl orthotitanate.
  • the aliphatic polycarboxylic acids and / or derivatives and the 2-methyl-butanediol-1,4 or mixtures of 2-methyl-butanediol-1,4 and polyhydric aliphatic alcohols in a molar ratio of 1: 1 to 1.8, preferably from 1: 1.05 to 1.2, catalyst-free or in the presence of esterification catalysts, advantageously in an atmosphere of inert gases such as nitrogen, helium, argon and others polycondensed in the melt at temperatures of 150 to 250 ° C, preferably 180 to 220 ° C, optionally under reduced pressure to the desired acid number, which is advantageously less than 2.
  • the esterification mixture is polycondensed at the above-mentioned temperatures up to an acid number of 80 to 30, preferably 40 to 30, under normal pressure and then under a pressure of less than 500 mbar, preferably from 50 to 150 mbar. This usually requires polycondensation times of 10 to 30 hours, preferably 15 to 20 hours.
  • polyester polyols according to the invention are used for the production of compact or cellular PU or PU-PH plastics by the polyisocyanate polyaddition process.
  • Suitable organic polyisocyanates are aliphatic, cycloaliphatic, araliphatic and preferably aromatic isocyanates.
  • alkylene diisocyanates with 4 to 12 carbon atoms in the alkylene radical, such as 1,12-dodecane diisocyanate, 1,4-tetramethylene diisocyanate and preferably 1,6-hexamethylene diisocyanate;
  • cycloaliphatic diisocyanates such as cyclohexane-1,3- and -1,4-diisocyanate and any mixtures of these isomers, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl-cyclohexane (isophorone diisocyanate), 2,4- and 2,6-hexahydrotoluylene diisocyanate and the corresponding isomer mixtures, 4,4 ⁇ -, 2,2 ⁇ - and 2,4 ⁇ -dicyclohexylmethane diisocyanate and
  • modified polyvalent isocyanates i.e. Products obtained by chemical reaction of the above di- and / or polyisocyanates are used.
  • suitable organic di- and polyisocyanates are: polyisocyanates containing carbodiimide groups according to DE-PS 10 92 007, polyisocyanates containing allophanate groups, such as those e.g. in British patent specification 994 890, the documents laid out in Belgian patent 761 626 and NL-OS 71 02 524, polyisocyanates containing isocyanurate groups, such as those e.g.
  • urethane-containing polyisocyanates such as those e.g. are described in the documents laid out in Belgian patent 752 261 or U.S. Patent 3,394,164, polyisocyanates containing acylated urea groups e.g. according to DE-PS 12 30 778, polyisocyanates containing biuret groups e.g. according to DE-PS 11 01 394 and GB-PS 889 050; polyisocyanates made by telomerization reaction e.g.
  • polyisocyanates containing ester groups such as those e.g. in GB-PS 965 474 and 1 072 956, US-PS 3 567 765 and DE-PS 12 31 688.
  • polyisocyanates containing urethane groups for example with low molecular weight linear or branched alkane diols, dialkylene glycols or polyoxyalkylene glycols with molecular weights up to 3000, based on ethylene oxide, 1,2-propylene oxide or mixtures thereof, modified 4,4′- and / or 2 , 4 ⁇ -diphenylmethane diiso polyisocyanates containing cyanate or 2,4- and / or 2,6-tolylene diisocyanate, carbodiimide groups and / or isocyanurate rings, for example 4,4′-, 2,4′-diphenylmethane diisocyanate-, 2,4- and / or 2, 6-tolylene diisocyanate base and in particular 4,4 ⁇ -diphenylmethane diisocyanate, mixtures of 2,4 ⁇ and 4,4 ⁇ -diphenylmethane diisocyanate, tolylene diisocyanates,
  • R1 is a hydrogen atom or a linear or branched alkyl radical having 1 to 12 carbon atoms, preferably 1 to 6 carbon atoms and R2 and R3 are identical or different, linear or branched alkyl radicals having 1 to 4 carbon atoms, such as, for example, a methyl, ethyl, Propyl, isopropyl, butyl or sec. Are butyl.
  • alkyl radicals R1 in which the branching point is located on the C1 carbon atom.
  • alkyl radicals R 1 may be mentioned, for example: methyl, ethyl, n and isopropyl, butyl, hexyl, octyl, decyl, 1-methyl-octyl, 2-ethyl-octyl, 1-methyl-hexyl-, 1,1-dimethyl-pentyl-, 1,3,3-trimethyl-hexyl-, 1-ethyl-pentyl-, 2-ethyl-pentyl- and preferably cyclohexyl-, 1-methyl- n-propyl, tert-butyl, 1-ethyl-n-propyl, 1-methyl-n-butyl and 1,1-dimethyl-n-propyl.
  • alkyl-substituted m-phenylenediamines are: 2,4-dimethyl, 2,4-diethyl, 2,4-diisopropyl, 2,4-diethyl-6-methyl, 2-methyl-4,6- diethyl-, 2,4,6-triethyl-, 2,4-dimethyl-6-cyclohexyl-, 2-cyclohexyl-4,6-diethyl-, 2-cyclohexyl-2,6-diisopropyl-, 2,4-dimethyl -6- (1-ethyl-n-propyl) -, 2,4-dimethyl-6- (1,1-dimethyl-n-propyl) - and 2- (1-methyl-n-butyl) -4.6 -dimethyl-phenylenediamine-1,3.
  • Alkyl-substituted diamino-diphenylmethanes such as e.g. 3,3 ⁇ -di- and 3,3 ⁇ , 5,5 ⁇ -tetra-n-alkyl-substituted 4,4 ⁇ -diamino-diphenylmethanes, e.g. 3,3 ⁇ -diethyl-, 3,3 ⁇ , 5,5 ⁇ -tetraethyl- and 3,3 ⁇ , 5,5 ⁇ -tetra-n-propyl-4,4 ⁇ -diamino-diphenylmethane.
  • Diamino-diphenylmethanes of the formula are advantageously used in which R4, R5, R6 and R7 are the same or different and represent a methyl, ethyl, propyl, isopropyl, sec-butyl and tert-butyl radical, but at least one of the radicals is an isopropyl or sec .-Butyl radical must be.
  • the alkyl-substituted 4,4'-diamino-diphenylmethane can also be mixed with isomers of the formulas are used, wherein R4, R5, R6 and R7 have the meaning given above.
  • Examples include: 3,3 ⁇ , 5-trimethyl-5 ⁇ -isopropyl-, 3,3 ⁇ , 5-triethyl-5 ⁇ -isopropyl-, 3,3 ⁇ , 5-trimethyl-5 ⁇ -sec-butyl-, 3,3 ⁇ , 5-triethyl-5 ⁇ -sec-butyl-4,4 ⁇ -diamino-diphenylmethane, 3,3 ⁇ -dimethyl-5,5 ⁇ -diisopropyl-, 3,3 ⁇ -diethyl-5,5 ⁇ -diisopropyl-, 3,3 ⁇ -dimethyl -5,5 ⁇ -di-sec-butyl-, 3,3 ⁇ -diethyl-5,5 ⁇ -di-sec.-butyl-, 3,5-dimethyl-3 ⁇ , 5 ⁇ -diisopropyl-, 3,5-diethyl- 3 ⁇ , 5 ⁇ -diisopropyl-, 3,5-dimethyl-3 ⁇ , 5 ⁇ -di-sec.-butyl-, 3,5-diethyl
  • the following primary aromatic diamines are preferably used: 2,4-diethyl-, 2,4-dimethyl-phenylenediamine-1,3, 2,4-diethyl-6-methyl-, 2-methyl-4,6-diethyl-phenylenediamine- 1,3, 2,4,6-triethyl-phenylenediamine-1,3, 2,4-dimethyl-6-tert-butyl-, 2,4-dimethyl-6-isooctyl- and 2,4-dimethyl-6 -cyclohexyl-phenylenediamine-1,3 and 3,5-dimethyl-3 ⁇ , 5 ⁇ -diisopropyl and 3,3 ⁇ , 5,5 ⁇ -tetraisopropyl-4,4 ⁇ -diamino-diphenylmethane.
  • the primary aromatic diamines (ci) can be used individually or in the form of mixtures, for example of alkyl-substituted 1,3-phenylenediamines, 3,3 ⁇ -di- and / or 3,3 ⁇ , 5,5 ⁇ -tetraalkyl-substituted 4,4 ⁇ -diamino-diphenylmethanes will.
  • secondary aromatic diamines (cii) are: N, N ⁇ -dialkyl-substituted aromatic diamines, which may optionally be substituted on the aromatic nucleus by alkyl radicals, having 1 to 20, preferably 1 to 4, carbon atoms in the N-alkyl radical, such as e.g.
  • Suitable polyhydric alcohols and / or polyoxyalkylene polyols are: aliphatic and / or araliphatic diols having 2 to 14, preferably 2 to 6 carbon atoms, such as 1,3-propanediol, 1,10-decanediol, diethylene glycol, dipropylene glycol , Bis (2-hydroxyethyl) hydroquinone and preferably ethylene glycol, 1,4-butanediol and 1,6-hexanediol, triols, such as glycerol and trimethylolpropane, and low molecular weight polyoxyalkylene polyols based on ethylene and / or 1,2-propylene oxide and the aforementioned starter molecules.
  • the chain extenders and / or crosslinking agents (c) can be added individually or in the form of mixtures and come, for example, in amounts of 5 to 50 parts by weight, preferably 10 to 40 parts by weight and in particular 15 to 30 parts by weight. based on 100 parts by weight of the polyester polyols (b), for use. If mixtures of sterically hindered primary aromatic diamines (ci) and sec. aromatic diamines (cii) and / or polyhydric alcohols (ciii) are used, these advantageously contain 1 to 40, preferably 5 to 20 parts by weight of components (cii) and / or per 100 parts by weight of component (ci) (ciii). Are never used as chain extenders in particular dermolecular diols (ciii) and / or aromatic diamines (ci), which contain at least one alkyl radical bonded ortho to the amino groups.
  • Organic metal compounds preferably organic tin compounds, such as tin (II) salts of organic carboxylic acids, e.g. Tin (II) acetate, Tin (II) octoate, Tin (II) ethylhexoate and Tin (II) laurate and the dialkyltin (IV) salts of organic carboxylic acids, e.g.
  • Dibutyltin diacetate, dibutyltin dilaurate, dibutyltin maleate and dioctyltin diacetate are used alone or preferably in combination with strongly basic amines.
  • Examples include amidines such as 2,3-dimethyl-3,4,5,6-tetrahydropyrimidine, tertiary amines such as triethylamine, tributylamine, dimethylbenzylamine, N-methyl-, N-ethyl-, N-cyclohexylmorpholine, N, N, N ⁇ , N ⁇ -tetramethylethylenediamine, N, N, N ⁇ , N ⁇ -tetramethyl-butanediamine.
  • Pentamethyl-diethylenetriamine tetramethyl-diaminoethyl ether, bis- (dimethylaminopropyl) urea, dimethylpiperazine, 1,2-dimethylimidazole, 1-aza-bicyclo- (3,3,0) -octane and preferably 1,4-diaza-bicyclo- ( 2,2,2) octane and alkanolamine compounds such as triethanolamine, triisopropanolamine, N-methyl- and N-ethyl-diethanolamine and dimethylethanolamine.
  • catalysts are: tris (dialkylaminoalkyl) -s-hexahydrotriazines, in particular tris (N, N-dimethylaminopropyl) -s-hexahydrotriazine, tetraalkylammonium hydroxides, such as tetramethylammonium hydroxide, alkali metal hydroxides, such as sodium hydroxide and alkali metal alcoholates, and potassium alkali metal alcoholates, such as sodium alkali metal alcoholate, and sodium alkali metal alcoholate, such as sodium methylate of long-chain fatty acids with 10 to 20 carbon atoms and optionally pendant OH groups.
  • 0.001 to 5% by weight, in particular 0.05 to 2% by weight, of catalyst or catalyst combination, based on the weight of component (b), are preferably used.
  • Blowing agents (e) which can be used to produce the cellular plastics or moldings include water which reacts with isocyanate groups to form carbon dioxide.
  • the amounts of water which can expediently be used are 0.5 to 2% by weight, based on the weight of component (b).
  • blowing agents that can be used are low-boiling liquids which evaporate under the influence of the exothermic polyaddition reaction.
  • Liquids which are compared to organic polyisocyanate are suitable are inert and have boiling points below 100 ° C.
  • examples of such, preferably used liquids are halogenated hydrocarbons, such as methylene chloride, trichlorofluoromethane, dichlorodifluoromethane, dichloromonomofluoromethane, dichlorotetrafluoroethane and 1,1,2-trichloro-1,2,2-trifluoroethane.
  • low-boiling liquid for the production of cell-containing PU or PU-PH moldings depends on the density that is to be achieved and, if appropriate, on the use of water. In general, amounts of 0.5 to 15 parts by weight, based on 100 parts by weight of component (b), give satisfactory results.
  • auxiliaries and / or additives (f) can also be incorporated into the reaction mixture.
  • auxiliaries and / or additives (f) can also be incorporated into the reaction mixture. Examples include surface-active substances, internal mold release agents, foam stabilizers, cell regulators, fillers, dyes, pigments, flame retardants, hydrolysis protection agents, fungistatic and bacteriostatic substances.
  • Suitable surface-active substances are compounds which serve to support the homogenization of the starting materials and, if appropriate, are also suitable for regulating the cell structure.
  • examples include emulsifiers, such as the sodium salts of castor oil sulfates or of fatty acids, and salts of fatty acids with amines, e.g. oleic acid diethylamine or stearic acid diethanolamine, salts of sulfonic acids, e.g.
  • Foam stabilizers such as siloxane-oxalkylene copolymers and other organopolysiloxanes, ethoxylated alkylphenols, ethoxylated fatty alcohols, paraffin oils, castor oil or castor esters and Turkish red oil and cell regulators, such as paraffins, fatty alcohols and dimethylpolysiloxanes.
  • the surface-active substances are usually used in amounts of 0.01 to 5 parts by weight, based on 100 parts by weight of component (b).
  • Suitable internal mold release agents are, for example, carboxylic acid esters and / or carboxamides which are prepared by esterification or amidation of a mixture of montanic acid and at least one aliphatic carboxylic acid with at least 10 carbon atoms with at least difunctional alkanolamines, polyols and / or polyamines with molecular weights from 60 to 400.
  • Fillers in particular reinforcing fillers, are to be understood as the conventional organic and inorganic fillers, reinforcing agents, weighting agents, agents for improving the abrasion behavior in paints, coating agents, etc., which are known per se.
  • examples include: inorganic fillers such as silicate minerals, for example layered silicates such as antigorite, serpentine, hornblende, amphibole, chrisotile, talc; Metal oxides such as kaolin, aluminum oxides, titanium oxides and iron oxides, metal salts such as chalk, heavy spar and inorganic pigments such as cadmium sulfide, zinc sulfide as well as glass, asbestos flour, etc.
  • inorganic fillers such as silicate minerals, for example layered silicates such as antigorite, serpentine, hornblende, amphibole, chrisotile, talc
  • Metal oxides such as kaolin, aluminum oxides, titanium oxides and iron oxides, metal salt
  • Kaolin china clay
  • aluminum silicate and coprecipitates of barium sulfate and aluminum silicate as well as natural and synthetic fibrous minerals, such as asbestos, wollastonite and in particular glass fibers of various lengths, which can optionally be sized.
  • suitable organic fillers are: coal, melamine, rosin, cyclopentadienyl resins and graft polymers based on styrene / acrylonitrile, which are obtained by in situ polymerization of acrylonitrile / styrene mixtures in polyetherols analogously to the information given in German patents 11 11 394, 12 22 669 (US 3 304 273, 3 383 351, 3 523 093), 11 52 536 (GB 1 040 452) and 11 52 537 (GB 987 618) and filler polyoxyalkylene polyols in which aqueous polymer dispersions are converted into polyoxyalkylene polyol dispersions .
  • the inorganic and organic fillers are advantageously incorporated into the reaction mixture in amounts of 0.5 to 50% by weight, preferably 1 to 40% by weight, based on the weight of components (a) to (c).
  • Suitable flame retardants are, for example, tricresyl phosphate, tris-2-chloroethyl phosphate, tris-chloropropyl phosphate and tris-2,3-dibromopropyl phosphate.
  • inorganic flame retardants such as aluminum oxide hydrate, antimony trioxide, arsenic oxide, ammonium polyphosphate and calcium sulfate, can also be used to flame retard the plastics or moldings.
  • inorganic flame retardants such as aluminum oxide hydrate, antimony trioxide, arsenic oxide, ammonium polyphosphate and calcium sulfate.
  • the organic polyisocyanates (a), polyester polyols (b) and chain extenders and / or crosslinking agents (c) are reacted in amounts such that the equivalence ratio of NCO -Groups of the polyisocyanates (a) to the sum of the reactive hydrogen atoms of components (b) and (c) 1: 0.85 to 1.25, preferably 1: 0.95 to 1.15.
  • the compact and preferably cell-containing moldings are produced by the prepolymer process or preferably by the one-shot process, PU moldings being expediently produced using the low-pressure technique and PU-PH moldings using the reaction injection molding technique.
  • the starting components can be fed individually and mixed intensively in the mixing chamber. It has proven to be particularly advantageous to work according to the two-component process and to dissolve the chain extenders and / or crosslinking agents (c) and catalysts (d) in the polyester polyols (b) and, if appropriate, with blowing agents (e), auxiliaries and / or to combine additives (f) in component (A) and to use the organic, optionally modified polyisocyanates as component (B). It is advantageous here, for example, that components (A) and (B) can be stored separately and transported in a space-saving manner and only have to be mixed in the appropriate amounts during processing.
  • the amount of the reaction mixture introduced into the mold is such that the compact moldings obtained have a density of 1.0 to 1.4 g / cm3, preferably of 1.0 to 1.2 g / cm3, and the cell-containing molded articles have a density of 0.2 to 1.1 g / cm 3, the microcellular molded articles preferably having a density of 0.8 to 1.0 g / cm 3, shoe soles preferably a density of 0.4 to 0.65 g / cm3 and foams preferably have a density of 0.25 to 0.4 g / cm3.
  • the starting components are introduced into the mold at a temperature of 15 to 80 ° C., preferably 20 to 60 ° C. and in particular 25 to 55 ° C.
  • the mold temperature is advantageously 20 to 100 ° C, preferably 30 to 80 ° C.
  • the degrees of compaction for the production of the microcellular or cellular moldings are between 1.1 and 8, preferably between 2 and 8.
  • the compact or cellular PU or PU-PH moldings obtained by the process according to the invention are particularly suitable for use in the automotive industry, for example as bumper covers, bumper guards and body parts such as gutters, fenders, spoilers and wheel arch extensions, and as technical housing parts, rollers and Shoe soles.
  • the foams are used, for example, as armrests, headrests, safety covers in the interior of automobiles and as motorcycle and bicycle saddles and cover layers in composite foams.
  • adipic acid 100 parts by weight of adipic acid, 31.1 parts by weight of ethanediol and 26.1 parts by weight of 2-methylbutanediol-1,4 were esterified under normal pressure and the water of condensation was distilled off at temperatures up to 220 ° C. The polycondensation was then brought to an end with the pressure being reduced to about 40 mbar.
  • the maximum soluble amount of blowing agent was determined in a characteristic rigid polyurethane foam formulation with variation of the polyester polyol, without the formulation becoming cloudy.
  • Prepolymer with an NCO content of 18.7 made from the ethanediol-2-methylbutanediol-1,4-polyadipate according to the invention and 4,4'-diphenylmethane diisocyanate.
  • component A 100 parts by weight of component A and 92.5 parts by weight of component B were mixed intensively at room temperature, introduced in a manner known per se into a metal mold at 40 ° C. and cured in the closed mold calmly. Because of the low viscosities of the polyester polyols according to the invention, equally good processing was possible using both the low-pressure and high-pressure processes.
  • the cellular polyurethane elastomers obtained were distinguished by excellent mechanical properties, in particular by low cold flexibility and very good stability to hydrolysis.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
EP87105757A 1986-04-25 1987-04-18 Polyesterpolyols liquides à température de chambre à base de 2-méthyl-butanediol-1,4, leur procédé de préparation et leur utilisation pour la préparation de matières plastiques par le procédé de polyaddition de polyisocyanate Withdrawn EP0248183A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19863614038 DE3614038A1 (de) 1986-04-25 1986-04-25 Bei raumtemperatur fluessige polyester-polyole auf basis von 2-methyl-butandiol-1,4, verfahren zu deren herstellung und deren verwendung zur herstellung von kunststoffen nach dem polyisocyanat-polyadditionsverfahren
DE3614038 1986-04-25

Publications (1)

Publication Number Publication Date
EP0248183A1 true EP0248183A1 (fr) 1987-12-09

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EP87105757A Withdrawn EP0248183A1 (fr) 1986-04-25 1987-04-18 Polyesterpolyols liquides à température de chambre à base de 2-méthyl-butanediol-1,4, leur procédé de préparation et leur utilisation pour la préparation de matières plastiques par le procédé de polyaddition de polyisocyanate

Country Status (4)

Country Link
US (1) US4731392A (fr)
EP (1) EP0248183A1 (fr)
CA (1) CA1274041A (fr)
DE (1) DE3614038A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0271788A3 (fr) * 1986-12-13 1989-03-15 BASF Aktiengesellschaft Procédé de préparation de mousses rigides contenant des groupes d'uréthane ou des groupes d'uréthane et d'isocyanurate ayant des cellules essentiellement fermées et leur utilisation
EP0271789A3 (fr) * 1986-12-13 1989-07-26 BASF Aktiengesellschaft Polyesterpolyols liquides à température ambiante à base de 2-méthylpentanediol-1,5, 2-éthylbutanediol-1,4, acide 2-méthylglutanique et/ou acide 2-éthylsuccinique ou dérivés formant ester, leur procédé de préparation et leur utilisation dans la préparation de résines d'après le procédé de polyaddition de polyisocyanates

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Publication number Priority date Publication date Assignee Title
DE3788063T2 (de) * 1987-01-22 1994-05-19 Kuraray Co Verfahren zur herstellung von polyurethanen.
CA2010561C (fr) * 1989-02-22 1995-04-04 Yasunobu Uchida Resine pour materiau composite antivibratoire, materiau antivibratoire composite obtenu a partir de ladite resine, et methode de fabrication du materiau antivibratoire
JP2660588B2 (ja) * 1989-11-30 1997-10-08 日本ポリウレタン工業株式会社 軟質ポリウレタン発泡体の製造方法
US5171758A (en) * 1990-03-12 1992-12-15 Olin Corporation Flame retardant urethane foams made using propylene oxide-based polyols
CA2107950C (fr) * 1992-10-22 2001-08-14 Bayer Corporation Stabilisation de systemes rim qui contiennent des additifs acides
JP3930089B2 (ja) * 1996-05-09 2007-06-13 株式会社イノアックコーポレーション 軟質ポリウレタンフォーム及びそれを用いたスピーカエッジ
BR0208342A (pt) 2001-04-06 2004-03-23 Basf Ag Processo para a preparação de produtos de poliadição de poliisocianato celular, e , produto de poliadição de poliisocianato celular.
US20070208096A1 (en) * 2006-03-02 2007-09-06 Oxid L.P. Sulfonated aromatic polyester polyol compositions
US20080114145A1 (en) * 2006-11-09 2008-05-15 Richard Czarnecki Self catalyzing polyurethanes
KR101657679B1 (ko) * 2009-12-24 2016-09-19 에스케이케미칼 주식회사 에스테르 폴리올의 제조방법
US9371410B2 (en) * 2013-09-16 2016-06-21 Dow Global Technologies Llc Polyurethane elastomers for use in subsea pipeline insulation
JP2024525806A (ja) * 2021-07-15 2024-07-12 ザ ライクラ カンパニー ユーケー リミテッド グリコールを含むコポリエステルポリオール及びコポリエステル、ならびにそれから製造されるポリウレタン及びスパンデックス

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GB781469A (en) * 1953-06-15 1957-08-21 Goodrich Co B F Improvements in or relating to rigid polyester-urethane thermoplastics
FR2147161A1 (fr) * 1971-07-26 1973-03-09 Du Pont
GB1475541A (en) * 1974-01-29 1977-06-01 Ici Ltd Polyurethane foams

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DE2045914B2 (de) * 1970-09-17 1975-11-27 Dynamit Nobel Ag, 5210 Troisdorf Verfahren zur Herstellung von linearen, hochmolekularen Polyestern

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB781469A (en) * 1953-06-15 1957-08-21 Goodrich Co B F Improvements in or relating to rigid polyester-urethane thermoplastics
FR2147161A1 (fr) * 1971-07-26 1973-03-09 Du Pont
GB1475541A (en) * 1974-01-29 1977-06-01 Ici Ltd Polyurethane foams

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0271788A3 (fr) * 1986-12-13 1989-03-15 BASF Aktiengesellschaft Procédé de préparation de mousses rigides contenant des groupes d'uréthane ou des groupes d'uréthane et d'isocyanurate ayant des cellules essentiellement fermées et leur utilisation
EP0271789A3 (fr) * 1986-12-13 1989-07-26 BASF Aktiengesellschaft Polyesterpolyols liquides à température ambiante à base de 2-méthylpentanediol-1,5, 2-éthylbutanediol-1,4, acide 2-méthylglutanique et/ou acide 2-éthylsuccinique ou dérivés formant ester, leur procédé de préparation et leur utilisation dans la préparation de résines d'après le procédé de polyaddition de polyisocyanates

Also Published As

Publication number Publication date
US4731392A (en) 1988-03-15
DE3614038A1 (de) 1987-11-05
CA1274041A (fr) 1990-09-11

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